http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-9914049-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1c584e230aa1949cab46ad03b9302519 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C271-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-46 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C269-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C271-28 |
| filingDate | 1999-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a819ed099ded96cfb65c28232e9867d0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88f2bf0fa4b825fc1748f280ef2e9f7b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b043e8de435c92f25d5669259f052460 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_475433b5bf1622705b41246c37ff2c07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_957364f6423bde8e50ba8a14ceb1add7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c95fe198a8a8b9fdccc0b36d117472b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7202afdede0e414dad0f89951e4f628c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8451aee89070c79aceff6a2b42cb184 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d94fde83161773ac30b6abe02c6c324 |
| publicationDate | 2001-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | BR-9914049-A |
| titleOfInvention | Optically active substituted N-aryl-o-aryloxy-alkyl-carbamates |
| abstract | Invention Patent: <B> "N-ARYL-O-ARYLoxy-ALKYL-CARBAMATES REPLACED OPTICALLY ACTIVE" <D>. The invention relates to new substituted N-aryl-O-aryloxy-alkyl-carbamates of the general formula (I), in which Ar¹ represents a monocyclic or bicyclic, carbocyclic or heterocyclic group, in each case possibly substituted, from the series phenyl, naphthyl, tetralinyl, furyl, benzofuryl, thienyl, benzothienyl, pyridinyl, quinolinyl, isoquinolinyl, or the group (a) hereinafter also possibly substituted, with A representing alkanodyly eventually substituted with halogen, with 1 to 3 carbon atoms , and the possible substituents in each case are preferably chosen from the following list: cyano, nitro, halogen, alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkyl-carbonyl, alkoxy-carbonyl, in each case eventually substituted with halogen, in each case with up to 5 carbon atoms, Ar² represents aryl with 6 or 10 carbon atoms, eventually replaced with nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, halogen or with (possibly substituted with cyan, halogen, C ~ 1 ~ -C ~ 4 ~ -alkoxy, C ~ 1 ~ -C ~ 4 ~ -alkyl, C ~ 1 ~ -C ~ 4 ~ -alkyl-sulfinyl or C ~ 1 ~ -C ~ 4 ~ -alkyl-sulfonyl) alkyl, alkoxy, alkylthio, alkyl-sulfinyl, alkyl-sulfonyl, alkyl-amino, dialkyl-amino, alkyl-carbonyl, alkoxy-carbonyl , alkyl-amino-carbonyl or dialkyl-amino-carbonyl with, in each case, up to 4 carbon atoms in the alkyl groups, R¹ represents alkyl with 1 to 4 carbon atoms eventually substituted with cyan, halogen or C ~ 1 ~ -C ~ 4 ~ -alkoxy, and R² represents hydrogen or alkyl with 1 to 4 carbon atoms eventually substituted with cyan, halogen or C ~ 1 ~ -C ~ 4 ~ -alkoxy, the substituents being on the carbon atom, to which R¹ is on, they are arranged in such a way that the plane of vibration of the polarized light is turned to the left, as well as processes for its preparation and use as a herbic gone. |
| priorityDate | 1998-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 37.